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Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress
BACKGROUND: The treatment of trigeminal neuralgia remains a challenging issue. Stem cells from human exfoliated deciduous teeth (SHED) provide optimized therapy for chronic pain. This study aimed to investigate the mechanisms underlying the attenuation of trigeminal neuralgia by SHED. METHODS: Trige...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pain Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530689/ https://www.ncbi.nlm.nih.gov/pubmed/36175337 http://dx.doi.org/10.3344/kjp.2022.35.4.383 |
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author | Yang, Zhijie Wang, Chun Zhang, Xia Li, Jing Zhang, Ziqi Tan, Zhao Wang, Junyi Zhang, Junyang Bai, Xiaofeng |
author_facet | Yang, Zhijie Wang, Chun Zhang, Xia Li, Jing Zhang, Ziqi Tan, Zhao Wang, Junyi Zhang, Junyang Bai, Xiaofeng |
author_sort | Yang, Zhijie |
collection | PubMed |
description | BACKGROUND: The treatment of trigeminal neuralgia remains a challenging issue. Stem cells from human exfoliated deciduous teeth (SHED) provide optimized therapy for chronic pain. This study aimed to investigate the mechanisms underlying the attenuation of trigeminal neuralgia by SHED. METHODS: Trigeminal neuralgia was induced by chronic constriction injury of the infraorbital nerve. The mechanical threshold was assessed after model establishment and local SHED transplantation. Endoplasmic reticulum (ER) morphology and Caspase12 expression in trigeminal ganglion (TG) was evaluated as well. BiP expression was observed in PC12 cells induced by tunicamycin. RESULTS: The local transplantation of SHED could relieve trigeminal neuralgia in rats. Further, transmission electron microscopy revealed swelling of the ER in rats with trigeminal neuralgia. Moreover, SHED inhibited the tunicamycin-induced up-regulated expression of BiP mRNA and protein in vitro. Additionally, SHED decreased the up-regulated expression of Caspase12 mRNA and protein in the TG of rats caused by trigeminal neuralgia after chronic constriction injury of the infraorbital nerve mode. CONCLUSIONS: This findings demonstrated that SHED could alleviate pain by relieving ER stress which provide potential basic evidence for clinical pain treatment. |
format | Online Article Text |
id | pubmed-9530689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95306892022-10-12 Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress Yang, Zhijie Wang, Chun Zhang, Xia Li, Jing Zhang, Ziqi Tan, Zhao Wang, Junyi Zhang, Junyang Bai, Xiaofeng Korean J Pain Experimental Research Articles BACKGROUND: The treatment of trigeminal neuralgia remains a challenging issue. Stem cells from human exfoliated deciduous teeth (SHED) provide optimized therapy for chronic pain. This study aimed to investigate the mechanisms underlying the attenuation of trigeminal neuralgia by SHED. METHODS: Trigeminal neuralgia was induced by chronic constriction injury of the infraorbital nerve. The mechanical threshold was assessed after model establishment and local SHED transplantation. Endoplasmic reticulum (ER) morphology and Caspase12 expression in trigeminal ganglion (TG) was evaluated as well. BiP expression was observed in PC12 cells induced by tunicamycin. RESULTS: The local transplantation of SHED could relieve trigeminal neuralgia in rats. Further, transmission electron microscopy revealed swelling of the ER in rats with trigeminal neuralgia. Moreover, SHED inhibited the tunicamycin-induced up-regulated expression of BiP mRNA and protein in vitro. Additionally, SHED decreased the up-regulated expression of Caspase12 mRNA and protein in the TG of rats caused by trigeminal neuralgia after chronic constriction injury of the infraorbital nerve mode. CONCLUSIONS: This findings demonstrated that SHED could alleviate pain by relieving ER stress which provide potential basic evidence for clinical pain treatment. The Korean Pain Society 2022-10-01 2022-10-01 /pmc/articles/PMC9530689/ /pubmed/36175337 http://dx.doi.org/10.3344/kjp.2022.35.4.383 Text en © The Korean Pain Society, 2022 https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Experimental Research Articles Yang, Zhijie Wang, Chun Zhang, Xia Li, Jing Zhang, Ziqi Tan, Zhao Wang, Junyi Zhang, Junyang Bai, Xiaofeng Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
title | Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
title_full | Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
title_fullStr | Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
title_full_unstemmed | Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
title_short | Stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
title_sort | stem cells from human exfoliated deciduous teeth attenuate trigeminal neuralgia in rats by inhibiting endoplasmic reticulum stress |
topic | Experimental Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530689/ https://www.ncbi.nlm.nih.gov/pubmed/36175337 http://dx.doi.org/10.3344/kjp.2022.35.4.383 |
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